A Study of Evacetrapib in Participants With Abnormal Cholesterol

Completed · Phase 1

Conditions studied: Dyslipidemia

In brief

The main purpose of this study is to measure how much of the drug gets into the blood stream and how long it takes the body to get rid of it when given once a day for 12, 24, and 52 weeks to participants with abnormal amounts of cholesterol and/or fat in the blood stream. Information about any side effects that may occur will also be collected. This study will also evaluate how the study drug reacts in the body when given once a day for 12, 24 and 52 weeks and how the body responds and returns to normal when the treatment is complete. The relationship between study drug and the results from the how the study drug reacts in the body may be explored, if needed.

Key facts

Study ID

NCT02168803

Run by

Eli Lilly and Company

People needed

101

Starts

2014-05-01

Expected to finish

2015-12-01

Last updated by the study team

2018-10-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Generally healthy participants or have stable medical conditions that, in the investigator's opinion, will not significantly alter the disposition of the drug, will not place the participant at increased risk by participating in the study, and will not interfere with interpretation of the data and meets one of the following criteria:
• Elevated low-density lipoprotein cholesterol (LDL-C) greater than 100 milligrams per deciliter (mg/dL), OR
• Low high-density lipoprotein cholesterol (HDL-C) less than 45 mg/dL (men); less than 50 mg/dL (women), OR
• Hypercholesterolemia on stable statin therapy for at least 3 month
• Have a body mass index (BMI) of 18 to 37 kilograms per square meter (kg/m\^2), inclusive, at screening

You may not qualify if…

• Have known allergies or intolerance to evacetrapib, related compounds
• Have history of recurrent rashes or chronic skin conditions
• Have significant history of or current chronic, active inflammatory conditions
• Have history or current evidence of significant neurological disorder
• Have long-standing diabetes that is insulin requiring
• Have history of or current symptoms of malabsorption syndromes, history of gastric bypass surgery

Where it is running

• Covance Clinical Research Inc — Daytona Beach, Florida, United States
• Covance — Dallas, Texas, United States
• Covance Clinical Research Inc — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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